Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 10
rs3810291
ZC3H4
19 47065746 3 prime UTR variant G/A snv 0.50 9
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs863750
ZNF664-RFLNA ; RFLNA
12 124020897 intron variant C/T snv 0.53 7
rs10132280 14 25458973 intergenic variant C/A snv 0.37 6
rs1358980
LOC105375070
6 43796814 intergenic variant C/T snv 0.40 6
rs1812175
HHIP-AS1 ; HHIP
4 144653692 intron variant A/G snv 0.79 6
rs395962
LIN28B
6 104949543 intron variant T/G snv 0.72 6
rs10804591 3 129615390 intergenic variant C/A snv 0.63 5
rs1167827
HIP1
7 75533848 3 prime UTR variant G/A snv 0.37 5
rs11878604 19 40827379 intron variant T/C snv 0.14 5
rs12902602
LOC112268142 ; CHRNB4
15 78675059 intron variant A/G snv 0.28 5
rs1884897 20 6632185 regulatory region variant A/G;T snv 5
rs2274432
TSEN15
1 184051811 missense variant G/A snv 0.33 0.28 5
rs2371767
ADAMTS9-AS2
3 64732582 intron variant G/C snv 0.38 5
rs2650492
SBK1
16 28322090 3 prime UTR variant G/A snv 0.20 5
rs2745353
RSPO3
6 127131790 intron variant C/T snv 0.55 5
rs6556301 5 177100576 downstream gene variant G/T snv 0.33 5
rs7536458 1 118321979 intergenic variant T/G snv 0.23 5
rs7801581
HOXA11-AS ; HOXA11
7 27184152 intron variant C/T snv 0.24 5
rs7970350
HMGA2
12 65966384 downstream gene variant C/T snv 0.48 5
rs905938
ZBTB7B ; DCST2
1 155018913 intron variant T/C snv 0.24 5
rs9991328
FAM13A
4 88791970 intron variant C/T snv 0.53 5
rs10245353 7 25818994 intergenic variant C/A snv 0.16 4